"Saibia" 3rd generation capillary electrophoresis instrument (unsterilized)
Taiwan·Risk Class 1·SEBIA·Registered Apr 10, 2015 – Apr 10, 2025Cancelled- Analysis ID
- 55531f6ffa5a80cc782acc8f65e83ea4
- Customs Code
- DHA09401509005
- Manufacturer
- SEBIA
- Manufacturer Country
- France
- Authorized Representative
- SCN TRADING COMPANY LIMITED
- Intended Use
- Limited to the first level identification scope of "Electrophoresis Equipment for Clinical Use (A.2485)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2485 Electrophoresis equipment for clinical use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Apr 10, 2015
- Expiry Date
- Apr 10, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Saibia" 3rd generation capillary electrophoresis instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55531f6ffa5a80cc782acc8f65e83ea4 and manufactured by SEBIA. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SEBIA, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.